Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
rs3318985190
- Species
- Rattus norvegicus
- Symbol
- rs3318985190
- Category
- Variant
- Variant type
- SNP
- Overlaps
- E2f8
- Location
- 1:98580994
- Nucleotide Change
- T>A
- Most Severe Consequence
- See all consequences
- intron variant
- HGVS.g name
- NC_051336.1:g.98580994T>A
- HGVS.c name
- ENSEMBL:ENSRNOT00000035512.7:c.294+106A>T
- RefSeq:NM_001100580.2:c.294+106A>T
- HGVS.p name
- Not Available
- Synonyms
- Not Available
- Notes
- Not Available
- Cross references
- Not Available
- References
- Not Available
- Genome location
- Chr1:98565717...98584265 (18.55 kb)
- Assembly version
- Not Available
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